Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients

Detalhes bibliográficos
Autor(a) principal: Silva,Gisleine Elisa Cavalcante da
Data de Publicação: 2006
Outros Autores: Assef,Abdol Hakin, Albino,Claudio Cordeiro, Ferri,Letícia de Araujo Funari, Tasin,Gilson, Takahashi,Mirian Hideko, Eik Filho,Wilson, Bazotte,Roberto Barbosa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Archives of Biology and Technology
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132006000500007
Resumo: The tolerability of stevioside (2.75 mg/kg/day) obtained from leaves of Stevia rebaudiana (Bert) Bertoni (Compositae) was investigated in hyperlipidemic patients. For this purpose a placebo controlled double blind study was performed. The patients were randomized in two groups: the first group received capsules containing placebo and the second group received capsules containing stevioside (50 mg) during 90 days. All capsules were ingested twice daily, i.e., 2 capsules before lunch and 2 capsules before dinner. After the selection of the patients and each 30 days body mass index and laboratory tests (alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, total cholesterol, high density lipoprotein, low density lipoprotein, very low density lipoprotein, triglycerides and glucose) were performed. Stevioside did not show any clinical relevant modification in all parameters investigated. Moreover the patients did not report severe adverse effect. Thus, we can concluded that stevioside, at least in the doses employed in this study was safe.
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spelling Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patientsStevia rebaudiana (Bert) Bertonisteviosideclinical investigationplacebo effectThe tolerability of stevioside (2.75 mg/kg/day) obtained from leaves of Stevia rebaudiana (Bert) Bertoni (Compositae) was investigated in hyperlipidemic patients. For this purpose a placebo controlled double blind study was performed. The patients were randomized in two groups: the first group received capsules containing placebo and the second group received capsules containing stevioside (50 mg) during 90 days. All capsules were ingested twice daily, i.e., 2 capsules before lunch and 2 capsules before dinner. After the selection of the patients and each 30 days body mass index and laboratory tests (alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, total cholesterol, high density lipoprotein, low density lipoprotein, very low density lipoprotein, triglycerides and glucose) were performed. Stevioside did not show any clinical relevant modification in all parameters investigated. Moreover the patients did not report severe adverse effect. Thus, we can concluded that stevioside, at least in the doses employed in this study was safe.Instituto de Tecnologia do Paraná - Tecpar2006-07-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132006000500007Brazilian Archives of Biology and Technology v.49 n.4 2006reponame:Brazilian Archives of Biology and Technologyinstname:Instituto de Tecnologia do Paraná (Tecpar)instacron:TECPAR10.1590/S1516-89132006000500007info:eu-repo/semantics/openAccessSilva,Gisleine Elisa Cavalcante daAssef,Abdol HakinAlbino,Claudio CordeiroFerri,Letícia de Araujo FunariTasin,GilsonTakahashi,Mirian HidekoEik Filho,WilsonBazotte,Roberto Barbosaeng2006-08-30T00:00:00Zoai:scielo:S1516-89132006000500007Revistahttps://www.scielo.br/j/babt/https://old.scielo.br/oai/scielo-oai.phpbabt@tecpar.br||babt@tecpar.br1678-43241516-8913opendoar:2006-08-30T00:00Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)false
dc.title.none.fl_str_mv Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
title Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
spellingShingle Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
Silva,Gisleine Elisa Cavalcante da
Stevia rebaudiana (Bert) Bertoni
stevioside
clinical investigation
placebo effect
title_short Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
title_full Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
title_fullStr Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
title_full_unstemmed Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
title_sort Investigation of the tolerability of oral stevioside in Brazilian hyperlipidemic patients
author Silva,Gisleine Elisa Cavalcante da
author_facet Silva,Gisleine Elisa Cavalcante da
Assef,Abdol Hakin
Albino,Claudio Cordeiro
Ferri,Letícia de Araujo Funari
Tasin,Gilson
Takahashi,Mirian Hideko
Eik Filho,Wilson
Bazotte,Roberto Barbosa
author_role author
author2 Assef,Abdol Hakin
Albino,Claudio Cordeiro
Ferri,Letícia de Araujo Funari
Tasin,Gilson
Takahashi,Mirian Hideko
Eik Filho,Wilson
Bazotte,Roberto Barbosa
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva,Gisleine Elisa Cavalcante da
Assef,Abdol Hakin
Albino,Claudio Cordeiro
Ferri,Letícia de Araujo Funari
Tasin,Gilson
Takahashi,Mirian Hideko
Eik Filho,Wilson
Bazotte,Roberto Barbosa
dc.subject.por.fl_str_mv Stevia rebaudiana (Bert) Bertoni
stevioside
clinical investigation
placebo effect
topic Stevia rebaudiana (Bert) Bertoni
stevioside
clinical investigation
placebo effect
description The tolerability of stevioside (2.75 mg/kg/day) obtained from leaves of Stevia rebaudiana (Bert) Bertoni (Compositae) was investigated in hyperlipidemic patients. For this purpose a placebo controlled double blind study was performed. The patients were randomized in two groups: the first group received capsules containing placebo and the second group received capsules containing stevioside (50 mg) during 90 days. All capsules were ingested twice daily, i.e., 2 capsules before lunch and 2 capsules before dinner. After the selection of the patients and each 30 days body mass index and laboratory tests (alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, total cholesterol, high density lipoprotein, low density lipoprotein, very low density lipoprotein, triglycerides and glucose) were performed. Stevioside did not show any clinical relevant modification in all parameters investigated. Moreover the patients did not report severe adverse effect. Thus, we can concluded that stevioside, at least in the doses employed in this study was safe.
publishDate 2006
dc.date.none.fl_str_mv 2006-07-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132006000500007
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132006000500007
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-89132006000500007
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
publisher.none.fl_str_mv Instituto de Tecnologia do Paraná - Tecpar
dc.source.none.fl_str_mv Brazilian Archives of Biology and Technology v.49 n.4 2006
reponame:Brazilian Archives of Biology and Technology
instname:Instituto de Tecnologia do Paraná (Tecpar)
instacron:TECPAR
instname_str Instituto de Tecnologia do Paraná (Tecpar)
instacron_str TECPAR
institution TECPAR
reponame_str Brazilian Archives of Biology and Technology
collection Brazilian Archives of Biology and Technology
repository.name.fl_str_mv Brazilian Archives of Biology and Technology - Instituto de Tecnologia do Paraná (Tecpar)
repository.mail.fl_str_mv babt@tecpar.br||babt@tecpar.br
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